Xu Tianqi, Yu Xi, Zhou Shenjun, Wu Yiwen, Deng Xinpeng, Wu Yuefei, Wang Shiyi, Gao Xiang, Nie Sheng, Zhou Chenhui, Sun Jie, Huang Yi
Department of Neurology, Ningbo First Hospital, Ningbo University, Ningbo, Zhejiang, China.
Key Laboratory of Precision Medicine for Atherosclerotic Diseases of Zhejiang Province, Ningbo, Zhejiang, China.
Front Genet. 2023 Jan 9;13:1079455. doi: 10.3389/fgene.2022.1079455. eCollection 2022.
We performed a case-control study to investigate the correlation between DNA methylation and mRNA expression of the glutathione S-transferase alpha 4 () gene and the risk of intracranial aneurysm (IA) in the Chinese Han population. After propensity score matching, 44 pairs of cases and controls were collected in this study. Fasting blood samples were collected for DNA and RNA extraction within 24 h of admission. Nine CpG dinucleotides were selected from the GSTA4 promoter region for DNA methylation pyrosequencing. mRNA expression of GSTA4 was measured by quantitative real-time polymerase chain reaction (RT-qPCR). cell experiments were conducted to verify the association between 5-aza-2'-deoxycytidine induced DNA hypomethylation and GSTA4 mRNA expression. The mean methylation level of GSTA4 was much lower in IA patients, especially in IA patients, especially in unruptured IA (UIA), than that in controls (IA vs. Control, < .001; ruptured IA (RIA) vs. Control, = .005; UIA vs. Control, < .001). With sex stratification, we further found that the association between GSTA4 methylation and IA risk presented only in women (mean methylation level: IA vs. Control, < .001; RIA vs. Control, = .009; UIA vs. Control, < .001). GSTA4 mRNA expression was significantly higher in the IA group than in the control group ( < .01) and negatively correlated with DNA methylation in all individuals (r = -.746, < .001). DNA hypomethylation can increase GSTA4 mRNA expression in human primary artery smooth muscle cells. The receiver operating characteristic (ROC) curve showed that GSTA4 mean methylation (AUC = .80, < .001) was a reliable predictor of women intracranial aneurysm, among which CpG 1 exhibited the best predictive value (AUC = .89, < .001). In addition, GSTA4 expression levels could also predict the risk of IA in women (AUC = .87, = .005). Decreased DNA methylation and increased mRNA expression of the GSTA4 gene are associated with the risk of IA in women.
我们开展了一项病例对照研究,以调查中国汉族人群中谷胱甘肽S-转移酶α4(GSTA4)基因的DNA甲基化与mRNA表达之间的相关性以及颅内动脉瘤(IA)的发病风险。经过倾向评分匹配后,本研究共收集了44对病例和对照。在入院后24小时内采集空腹血样用于DNA和RNA提取。从GSTA4启动子区域选择9个CpG二核苷酸进行DNA甲基化焦磷酸测序。通过定量实时聚合酶链反应(RT-qPCR)检测GSTA4的mRNA表达。进行细胞实验以验证5-氮杂-2'-脱氧胞苷诱导的DNA低甲基化与GSTA4 mRNA表达之间的关联。IA患者中GSTA4的平均甲基化水平远低于对照组,尤其是未破裂IA(UIA)患者(IA组与对照组相比,P<0.001;破裂IA(RIA)组与对照组相比,P = 0.005;UIA组与对照组相比,P<0.001)。按性别分层后,我们进一步发现GSTA4甲基化与IA风险之间的关联仅在女性中存在(平均甲基化水平:IA组与对照组相比,P<0.001;RIA组与对照组相比,P = 0.009;UIA组与对照组相比,P<0.001)。IA组中GSTA4的mRNA表达显著高于对照组(P<0.01),且在所有个体中与DNA甲基化呈负相关(r = -0.746,P<0.001)。DNA低甲基化可增加人原代动脉平滑肌细胞中GSTA4的mRNA表达。受试者工作特征(ROC)曲线显示,GSTA4平均甲基化(AUC = 0.80,P<0.001)是女性颅内动脉瘤的可靠预测指标,其中CpG 1表现出最佳预测价值(AUC = 0.89,P<0.001)。此外,GSTA4表达水平也可预测女性IA的风险(AUC = 0.87,P = 0.005)。GSTA4基因DNA甲基化降低和mRNA表达增加与女性IA风险相关。